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Automatic thalamus and hippocampus segmentation from MP2RAGE: comparison of publicly available methods and implications for DTI quantification

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Automatic thalamus and hippocampus segmentation from MP2RAGE: comparison of publicly available methods and implications for DTI quantification

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dc.contributor.author Naess-Schmidt, Erhard es_ES
dc.contributor.author Tietze, Anna es_ES
dc.contributor.author Blicher, Jakob Udby es_ES
dc.contributor.author Petersen, Mikkel es_ES
dc.contributor.author Mikkelsen, Irene K. es_ES
dc.contributor.author Coupe, Pierrick es_ES
dc.contributor.author Manjón Herrera, José Vicente es_ES
dc.contributor.author Eskildsen, Simon Fristed es_ES
dc.date.accessioned 2017-05-29T07:39:09Z
dc.date.available 2017-05-29T07:39:09Z
dc.date.issued 2016-11
dc.identifier.issn 1861-6410
dc.identifier.uri http://hdl.handle.net/10251/81872
dc.description.abstract Purpose In both structural and functional MRI, there is a need for accurate and reliable automatic segmentation of brain regions. Inconsistent segmentation reduces sensitivity and may bias results in clinical studies. The current study compares the performance of publicly available segmentation tools and their impact on diffusion quantification, emphasizing the importance of using recently developed segmentation algorithms and imaging techniques. Methods Four publicly available, automatic segmentation methods (volBrain, FSL, FreeSurfer and SPM) are compared to manual segmentation of the thalamus and hippocampus imaged with a recently proposed T1-weighted MRI sequence (MP2RAGE). We evaluate morphometric accuracy on 22 healthy subjects and impact on diffusivity measurements obtained from aligned diffusion-weighted images on a subset of 10 subjects. Results Compared to manual segmentation, the highest Dice similarity index of the thalamus is obtained with volBrain using a local library (M = 0.913, SD = 0.014) followed by volBrain using an external library (M = 0.868, SD = 0.024), FSL (M = 0.806, SD = 0.034), FreeSurfer (M = 0.798, SD = 0.049) and SPM (M = 0.787, SD = 0.031). The same order is found for hippocampus with volBrain local (M = 0.892, SD = 0.016), volBrain external (M = 0.859, SD = 0.014), FSL (M = 0.808, SD = 0.017), FreeSurfer (M = 0.771, SD = 0.023) and SPM (M = 0.735, SD = 0.038). For diffusivity measurements, volBrain provides values closest to those obtained from manual segmentations. volBrain is the only method where FA values do not differ significantly from manual segmentation of the thalamus. Conclusions Overall we find that volBrain is superior in thalamus and hippocampus segmentation compared to FSL, FreeSurfer and SPM. Furthermore, the choice of segmentation technique and training library affects quantitative results from diffusivity measures in thalamus and hippocampus. es_ES
dc.description.sponsorship This work was funded in part by MINDLab UNIK initiative at Aarhus University, funded by the Danish Ministry of Science, Technology and Innovation, Grant Agreement Number 09065250, partly by the Spanish grant TIN2013-43457-R from the Ministerio de Economia competitividad and with financial support from the French State, managed by the French National Research Agency (ANR) in the frame of the Investments for the future Programme IdEx Bordeaux (ANR-10-IDEX-03-02) by funding HL-DTI grant, Cluster of excellence CPU, LaBEX TRAIL (HR-DTI ANR-10-LABX-57) and the CNRS multidisciplinary project "Defi ImagIn". en_EN
dc.language Inglés es_ES
dc.publisher Springer Verlag (Germany) es_ES
dc.relation.ispartof International Journal of Computer Assisted Radiology and Surgery es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject MRI es_ES
dc.subject Segmentation es_ES
dc.subject Hippocampus es_ES
dc.subject Thalamus es_ES
dc.subject MP2RAGE es_ES
dc.subject Diffusion-weighted imaging es_ES
dc.subject.classification FISICA APLICADA es_ES
dc.title Automatic thalamus and hippocampus segmentation from MP2RAGE: comparison of publicly available methods and implications for DTI quantification es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1007/s11548-016-1433-0
dc.relation.projectID info:eu-repo/grantAgreement/Ministry of Higher Education and Science//9065250/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/ANR//ANR-10-LABX-0057/FR/Translational Research and Advanced Imaging Laboratory/TRAIL/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/ANR//ANR-10-IDEX-0003/FR/Initiative d’excellence de l’Université de Bordeaux/IDEX BORDEAUX/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MINECO//TIN2013-43457-R/ES/CARACTERIZACION DE FIRMAS BIOLOGICAS DE GLIOBLASTOMAS MEDIANTE MODELOS NO-SUPERVISADOS DE PREDICCION ESTRUCTURADA BASADOS EN BIOMARCADORES DE IMAGEN/ es_ES
dc.rights.accessRights Cerrado es_ES
dc.contributor.affiliation Universitat Politècnica de València. Escola Tècnica Superior d'Enginyeria Informàtica es_ES
dc.description.bibliographicCitation Naess-Schmidt, E.; Tietze, A.; Blicher, JU.; Petersen, M.; Mikkelsen, IK.; Coupe, P.; Manjón Herrera, JV.... (2016). Automatic thalamus and hippocampus segmentation from MP2RAGE: comparison of publicly available methods and implications for DTI quantification. International Journal of Computer Assisted Radiology and Surgery. 11(11):1979-1991. https://doi.org/10.1007/s11548-016-1433-0 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://link.springer.com/article/10.1007/s11548-016-1433-0 es_ES
dc.description.upvformatpinicio 1979 es_ES
dc.description.upvformatpfin 1991 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 11 es_ES
dc.description.issue 11 es_ES
dc.relation.senia 329838 es_ES
dc.contributor.funder Ministerio de Economía y Competitividad es_ES
dc.contributor.funder Ministry of Higher Education and Science, Dinamarca es_ES
dc.contributor.funder Agence Nationale de la Recherche, Francia es_ES
dc.contributor.funder Centre National de la Recherche Scientifique, Francia es_ES
dc.contributor.funder Aarhus University
dc.description.references Mulder ER, de Jong RA, Knol DL, van Schijndel RA, Cover KS, Visser PJ, Barkhof F, Vrenken H (2014) Hippocampal volume change measurement: quantitative assessment of the reproducibility of expert manual outlining and the automated methods FreeSurfer and FIRST. Neuroimage 92:169–181 es_ES
dc.description.references Heckemann RA, Hajnal JV, Aljabar P, Rueckert D, Hammers A (2006) Automatic anatomical brain MRI segmentation combining label propagation and decision fusion. Neuroimage 33(1):115–126 es_ES
dc.description.references Rohlfing T, Brandt R, Menzel R, Maurer CR (2004) Evaluation of atlas selection strategies for atlas-based image segmentation with application to confocal microscopy images of bee brains. Neuroimage 21(4):1428–1442 es_ES
dc.description.references Aljabar P, Heckemann RA, Hammers A, Hajnal JV, Rueckert D (2009) Multi-atlas based segmentation of brain images: atlas selection and its effect on accuracy. Neuroimage 46(3):726–738 es_ES
dc.description.references Coupé P, Manjón JV, Fonov V, Pruessner J, Robles M, Collins DL (2011) Patch-based segmentation using expert priors: application to hippocampus and ventricle segmentation. Neuroimage 54(2):940–954 es_ES
dc.description.references Tong T, Wolz R, Coupé P, Hajnal JV, Rueckert D (2013) Segmentation of MR images via discriminative dictionary learning and sparse coding: application to hippocampus labeling. Neuroimage 76:11–23 es_ES
dc.description.references Eskildsen SF, Coupé P, Fonov V, Manjón JV, Leung KK, Guizard N, Wassef SN, Østergaard LR, Collins DL (2012) BEaST: brain extraction based on nonlocal segmentation technique. Neuroimage 59(3):2362–2373 es_ES
dc.description.references Falangola MF, Jensen JH, Tabesh A, Hu C, Deardorff RL, Babb JS, Ferris S, Helpern JA (2013) Non-Gaussian diffusion MRI assessment of brain microstructure in mild cognitive impairment and Alzheimer’s disease. Magn Reson Imaging 31(6):840–846 es_ES
dc.description.references Mitchell AS, Sherman SM, Sommer MA, Mair RG, Vertes RP, Chudasama Y (2014) Advances in understanding mechanisms of thalamic relays in cognition and behavior. J Neurosci 34(46):15340–15346 es_ES
dc.description.references Vestergaard-Poulsen P, Wegener G, Hansen B, Bjarkam CR, Blackband SJ, Nielsen NC, Jespersen SN (2011) Diffusion-weighted MRI and quantitative biophysical modeling of hippocampal neurite loss in chronic stress. PLoS ONE 6(7):e20653 es_ES
dc.description.references Granziera C, Daducci A, Romascano D, Roche A, Helms G, Krueger G, Hadjikhani N (2014) Structural abnormalities in the thalamus of migraineurs with aura: a multiparametric study at 3 T. Hum Brain Mapp 35(4):1461–1468 es_ES
dc.description.references Coupé P, Eskildsen SF, Manjón JV, Fonov VS, Collins DL (2012) Simultaneous segmentation and grading of anatomical structures for patient’s classification: application to Alzheimer’s disease. Neuroimage 59(4):3736–3747 es_ES
dc.description.references Marques JP, Kober T, Krueger G, van der Zwaag W, Van de Moortele PFF, Gruetter R (2010) MP2RAGE, a self bias-field corrected sequence for improved segmentation and T1-mapping at high field. Neuroimage 49(2):1271–1281 es_ES
dc.description.references Fujimoto K, Polimeni JR, van der Kouwe AJW, Reuter M, Kober T, Benner T, Fischl B, Wald LL (2014) Quantitative comparison of cortical surface reconstructions from MP2RAGE and multi-echo MPRAGE data at 3 and 7 T. Neuroimage 90:60–73 es_ES
dc.description.references Dudo RO, Hart PE, Stork D (2001) Pattern classification, 2nd edn. Wiley, Hoboken es_ES
dc.description.references Leemans A, Jeurissen B, Sijbers J, Jones D (2009) ExploreDTI: a graphical toolbox for processing, analyzing, and visualizing diffusion MR data. In: Proceedings 17th scientific meeting, international society for magnetic resonance in medicine, vol 17, no 2, p 3537 es_ES
dc.description.references Yushkevich PA, Piven J, Hazlett HC, Smith RG, Ho S, Gee JC, Gerig G (2006) User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability. Neuroimage 31(3):1116–1128 es_ES
dc.description.references Power BD, Wilkes FA, Hunter-Dickson M, van Westen D, Santillo AF, Walterfang M, Nilsson C, Velakoulis D, Looi JCL (2015) Validation of a protocol for manual segmentation of the thalamus on magnetic resonance imaging scans. Psychiatry Res 232(1):98–105 es_ES
dc.description.references Boccardi M, Bocchetta M, Apostolova LG, Barnes J, Bartzokis G, Corbetta G,DeCarliC, deToledo-Morrell L, Firbank M, Ganzola R, Gerritsen L, Henneman W, Killiany RJ, Malykhin N, Pasqualetti P, Pruessner JC, Redolfi A, Robitaille N, Soininen H, Tolomeo D, Wang L, Watson C, Wolf H, Duvernoy H, Duchesne S, Jack CR, Frisoni GB (2014) Delphi definition of the EADC-ADNI harmonized protocol for hippocampal segmentation on magnetic resonance. Alzheimers Dement 11(2):126–138 es_ES
dc.description.references Manjón JV, Coupé P (2015) volBrain: an online MRI brain volumetry system. Hum Brain Mapp 15:2015 es_ES
dc.description.references Patenaude B, Smith SM, Kennedy DN, Jenkinson M (2011) A Bayesian model of shape and appearance for subcortical brain segmentation. Neuroimage 56(3):907–922 es_ES
dc.description.references Fischl B, Salat DH, Busa E, Albert M, Dieterich M, Haselgrove C, Van Der Kouwe A, Killiany R, Kennedy D, Klaveness S, Montillo A, Makris N, Rosen B, Dale AM (2002) Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain. Neuron 33(3):341–355 es_ES
dc.description.references Ashburner J, Friston KJ (2005) Unified segmentation. Neuroimage 26(3):839–851 es_ES
dc.description.references Frisoni GB, Jack CR, Bocchetta M, Bauer C, Frederiksen KS, Liu Y, Preboske G, Swihart T, Blair M, Cavedo E, Grothe MJ, Lanfredi M, Martinez O, Nishikawa M, Portegies M, Stoub T, Ward C, Apostolova LG, Ganzola R, Wolf D, Barkhof F, Bartzokis G, DeCarli C, Csernansky JG, Detoledo-Morrell L, Geerlings MI, Kaye J, Killiany RJ, Lehericy S, Matsuda H, O’Brien J, Silbert LC, Scheltens P, Soininen H, Teipel S, Waldemar G, Fellgiebel A, Barnes J, Firbank M, Gerritsen L, Henneman W, Malykhin N, Pruessner JC, Wang L, Watsonl C, Wolf H, Deleon M, Pantel J, Ferrari C, Bosco P, Pasqualetti P, Duchesne S, Duvernoy H, Boccardi M, Albert MS, Bennet D, Camicioli R, Collins DL, Dubois B, Hampel H, Denheijer T, Hock C, Jagust W, Launer L, Maller JJ, Mueller S, Sachdev P, Simmons A, Thompson PM, Visser PJ, Wahlund LO, Weiner MW, Winblad B (2015) The EADC-ADNI harmonized protocol for manual hippocampal segmentation on magnetic resonance: evidence of validity. Alzheimer’s Dement 11(2):111–125 es_ES
dc.description.references Næss-Schmidt ET, Tietze A, Mikkelsen IK, Petersen M, Blicher JU, Coupé P, Manjón JV, Eskildsen SF (2015) Patch-based segmentation from MP2RAGE images: comparison to conventional techniques. In: Wu G, Coupé P, Zhan Y, Munsell B, Rueckert D (eds) First international workshop, patch-techniques in medical imaging. Lecture notes in computer science, held in conjunction with MICCAI 2015, vol 9467. Munich, Germany, pp.180–187 es_ES
dc.description.references Barbagallo G, Nicoletti G, Cherubini A, Trotta M, Tallarico T, Chiriaco C, Nisticò R, Salvino D, Bono F, Valentino P, Quattrone A (2014) Diffusion tensor MRI changes in gray structures of the frontal-subcortical circuits in amyotrophic lateral sclerosis. Neurol Sci 35(6):911–918 es_ES
dc.description.references Okubo G, Okada T, Yamamoto A, KanagakiM, Fushimi Y, Okada T, Murata K, Togashi K (2015) MP2RAGE for deep gray matter measurement of the brain: a comparative study with MPRAGE. J Magn Reson Imaging 43(1):55–62 es_ES


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